US3063956A - Polyester solution in an aromatic ether solvent - Google Patents
Polyester solution in an aromatic ether solvent Download PDFInfo
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- US3063956A US3063956A US765024A US76502458A US3063956A US 3063956 A US3063956 A US 3063956A US 765024 A US765024 A US 765024A US 76502458 A US76502458 A US 76502458A US 3063956 A US3063956 A US 3063956A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
- C08J3/091—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids characterised by the chemical constitution of the organic liquid
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/62—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyesters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2367/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
Definitions
- This invention relates to new compositions of matter and more particularly to new and useful compositions of matter comprising solutions or dopes of synthetic linear condensation polyesters. It is further concerned with new compositions of matter which are capable of being formed into useful articles such as ribbons, films, bristles, fibers, filaments and the like.
- melt-spinning comprises melting chips of a polyester on a heated grid and passing the melt through .a filter bed of small particles, such as sand, and the like. Subsequently, the melt is forced through a spinneret and the filaments so formed are cooled.
- melt-spinning has certain disadvantages such as the employment of high temperatures which makes the addition of plasticizers and modifying agents difiicult, because there is a tendency for the added agents to discolor and decompose.
- the polyester is dissolved in a solvent therefor and extruded through a spinneret in the usual manner.
- the solution is extruded into an atmosphere of inert gas which may be heated.
- the motion of the inert gaseous atmosphere, the extruded fiber and the application of heat all aid in disposing of the volatile solvent.
- the wet-spinning method in which a solution of polyester is extruded into a bath containing a non-solvent for the polyester has a number of advantages over the melt-spinning method.
- the wet-spinning method is generally more economical and can be carried out at lower temperatures. Therefore, plasticizers and other agents may be added with a minimum tendency toward discoloration and decomposition.
- certain types of plasticizers and modifying agents tend to be less compatible for blending in a melt at high temperatures, whereas they can be readily incorporated in a polyester solution at a low temperature. Solutions offer the further advantage in that they may be easily cast into films or coatings of uniform thickness. This is extremely diflicult with a molten composition because of its relatively high viscosity.
- polyesters are insoluble in the more common organic solvents. From the standpoint of low cost, solvent power, non-corrosiveness and ease of recovery, there is a scarcity of suitable solvents for the more usual types of polyesters.
- the principal object of the instant invention is the preparation of polyester solutions or dopes which are capable of being transformed into shaped articles.
- Another object is to provide synthetic linear condensation polyester compositions in solutions which are stable and have non-gelation characteristics.
- Another object of the invention is to prepare spinnable solutions of polyester compositions.
- x is NH or a halogen.
- ortho-anisidine p-chloroanisole, m-anisidine, p-anisidine, o-chl-oroanisole, o-bromoanisole, and p-bromoanisole.
- Solutions of high solids content and good stability can be prepared by mixing the polyester in the compounds mentioned hereinabove and heating to a temperature in a range of C. to the boiling point of the mixture. If desired, the mixture may be stirred while heating. However, stirring is not necessary to eifect solution, although it has been found that the polyester goes into solution more smoothly and evenly and with a greater rate of speed when stirring is employed. Whether stirring is employed or not, a miscible mixture of the synthetic linear condensation polyester is attained.
- the maximum solids concentration of the polyester that can be obtained in the solution and the viscosity of the solution depend upon the nature of the polyester, the solvent mixture and the temperature. In the manufacture of filaments and fibers a polyester having a molecular weight of at least 10,000 is employed in making a solution.
- Lower molecular weight polyesters may be utilized when the solution to be formed is to be used as a coating or as a lacquer.
- prapering solutions or dopes suitable for spinning into filaments and fibers 10 to 20 percent by weight of the polyester, based on the total weight of the solution, is suitable.
- R is an alkyl group containing from 2 to 6 carbon atoms, for example, tn'methylol ethane, trimethylol propane, and like compounds up to trimethylol hexane; and the compounds having the formula:
- Aromatic polyfunctional acid esters may also be employed in this invention as chain-branching agents and particularly those having the formula:
- T he chain-branching agents or cross-linking agents may be employed in the preparation of the polyesters and copolyesters in amounts ranging from 0.05 mol percent to 2.4 mol percent, based on the amount of dicarboxylic acid or dialkyl ester thereof employed in the reaction mixture.
- the preferred range of chain-branching agent for use in the present invention is from 0.1 to 1.0 mol percent.
- the reaction is conducted at reduced pressures and preferably in the presence of an inert gas, such as nitrogen, in order to prevent oxidation.
- an inert gas such as nitrogen
- a pressure within the range of less than 1 mm. up to 5 mm. of mercury is employed.
- This reduced pressure is necessary to remove the free ethylene glycol that is formed during this stage of the reaction, the ethylene glycol being volatilized under these conditions and removed from the system.
- the polymerization step is c0nducted at a temperature in the range of 220 to 300 C.
- This stage of the reaction may be effected either in the liquid, melt or solid phase. In the liquid phase, particularly, reduced pressures must be employed in order to remove the free ethylene glycol which emerges from the polymer as a result of the condensation reaction.
- the modified linear condensation polyesters produced in accordance with the present invention, have a specific viscosity in the range of 0.30 to 0.60, which represents the fiberand filament-forming polymers. It is to be understood, of course, that non-fiber-forming polyesters may be produced by means of the present invention, which have a specific viscosity greater or less than that reiterated above and such polyesters are useful, for example, in the manufacture of coating compositions, lacquers, molding compositions, and the like. This specific viscosity range and variations thereof also are applicable to the unmodified polyesters, such as polyethylene terephthalate.
- the specific viscosity range of the fiber-forming polymers that is, from 0.3 to about 0.6, indicates high molecular weight polymers of from about 10,000 to about 50,000 molecular weight.
- polyester solutions of the present invention which have a modified appearance or modified properties
- various agents to accomplish these effects may be added to the polyester solutions of this invention prior to the fabrication of the articles without any ill efiects thereon.
- Such added agents might be plasticizers, pigments, dyes, anti-static agents, fire-retarding agents, etc.
- Example I 9 grams of o-anisidine and 1 gram of polyethylene terephthalate were mixed together and warmed with stirring to 180 C. where the polymer readily dissolved yielding a clear fluid solution suitable for both wet and dry spinning. On cooling, the solution solidified at 85 C. but was easily redissolved upon the application of heat.
- Example 11 There was charged to a reaction vessel 82 grams of dimethyl terephthalate, 106.2 grams of ethylene glycol (approximately 88 ml.) and 8.2 grams of ethoxypolyethylene glycol having an average molecular weight of about 3050 (0.5 mol percent based on the mols of dimethyl terephthalate). Subsequently, 40 mg. of manganous formate was added to the reaction vessel. The reactants were Will mixed and heated at 177 C. until solution was effected. The mixture was maintained at this temperature for 90 minutes to bring about the ester'interchange reaction. Thereafter, the temperature was raised to 225 C. to remove excess ethylene glycol and maintained at that temperature under a vacuum of less than 1 mm.
- Example III 9 grams of p-chloroanisole and 1 gram of polyethylene terephthalate were mixed together and warmed with stirring to 185 C. where the polymer readily dissolved yielding a clear fluid solution suitable for both wet and dry spinning. On cooling, the solution solidified at C. but was easily redissolved upon the application of heat.
- Example IV A polyester formed as in Example II but with approximately 16.4 grams of ethoxypolyethylene glycol (that is, about 1 mol percent based on the rmols of dimethyl terephthalate) were mixed with 9 grams of p-chloroanisole and warmed with stirring to 185 C. where the polymer readily dissolved yielding a clear fluid solution. On cooling, the solution became solid at about 125 C. but was easily redissolved upon the application of heat.
- ethoxypolyethylene glycol that is, about 1 mol percent based on the rmols of dimethyl terephthalate
- Example V 9 grams of o-anisidine and 1 gram of the polyester employed in Example IV were mixed together and warmed with stirring to 180 C. where the polymer readily dissolved yielding a clear fluid solution suitable for both Wet and dry spinning. The solution was stable at temperatures above 85 C.
- Example VII There was charged to a reaction vessel 1650 grams of dimethyl terephthalate, 1980 grams (approximately 1775 ml.) of ethylene glycol and 165 grams of methoxypolyethylene glycol having an average molecular Weight of abopt 2000 (1.0 mol percent based on the mols of dimethyl terephthalate). There was also added to the reaction vessel 1.32 grams of pentaerythritol. Subse, quently, 1.07 grams of zinc acetylacetonate were added to the reaction vessel. The reactants were well mixed and heated for about 90 minutes at atmospheric pressure and at a temperature gradually raised from C. to 198 C. until solution was effected.
- Example VIII 2 grams of the polyester prepared in Example ViI were mixed with 8 grams of p-chloroanisole. The polyester was practically completely dissolved at about 175 C. The solution so formed was very viscous and suitable for the preparation of films.
- Example IX 2 grams of the polyester formed by the procedure of Example VII were mixed with 8 grams of o-anisidine.
- the polyester began to dissolve at about 140 C.
- Solution was complete at 170 C.
- the solution became turbid and thick.
- the solution was clear, colorless and viscous. It was suitable for the formation of fibers.
- Example X 2.5 grams of the polyester prepared according to the procedure of Example VII and 7.0 grams of o-anisidine were mixed together and heated with stirring to about 170 C. where solution was formed. Upon cooling, precipitation of the polyester was noted at about 155 C. At 140 C. the solution became turbid and thick and at 135 C. it was semi-solid. The solution was suitable for the formation of films at about 170 C.
- polyester compositions of this invention can be usefully employed in the coating field, for example, in the coating of textile fabrics.
- a fabric can be coated and/or impregnated with the polyester solutions described herein and then treated, that is soaked, in a non-solvent for the polyester in order to precipitate the polyester in and on the fabric.
- Metals, paper and impervious films may also be coated with the polyester compositions of this invention by conventional and wellknown procedures.
- One of the principal advantages of the instant invention is that it provides polyester compositions which are readily convertible to useful shaped articles by the wet or dry spinning methods which are more economical than the melt-spinning method. Numerous other advantages of this invention will be apparent to those skilled in the art from reading the instant description.
- a new composition of matter comprising a solution of a synthetic linear condensation polyester dissolved in a solvent having the general formula
- R is selected from the group consisting of alkyl groups containing 1 to 18 carbon atoms and aryl groups containing 6 to 10 carbon atoms, In and n are integers from 2 to 22, and x is an integer from 1 to 100, and (C) the polyesters of (B) containing 0.05 mol percent to 4.0 mol percent of a chain terminator based on the total weight of said dicarboxylic acid modified by 0.05 mol percent to 2.4 mol percent based on the total weight of said dicarboxylic acid, of a chain-branching agent comprising pentaerythritol.
- a new composition of matter as defined in claim 1 wherein the chain terminator is methoxypolyethylene glycol.
- a new composition of matter as defined in claim 1 wherein the cross-linking agent is pentaerythritol.
- a new composition of matter comprising a solution of a synthetic linear condensation polyester dissolved in a solvent having the general formula,
- x is selected from the group consisting of -NH and chloro
- said polyester being selected from the group consisting of (A) polyesters formed by the reaction of at least one dicarboxylic acid selected from the group consisting of aromatic dicarboxylic acids and saturated aliphatic dicarboxylic acids and at least one glycol of the series HO(CH OI-I wherein n is an integer from 2 to 10, (B) the polyesters of (A) modified by 0.05 mol percent to 1.0 mol percent, based on the total weight of said dicarboxylic acid, of a chain terminator having the formula,
- x is selected from the group consisting of NH and chloro.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
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Description
United States Patent OfiC 3,053,956 Patented Nov. 13, 1962 No Drawing. Filed -Oct. 3, 1958, Ser. No. 765,024 13 Claims. (Cl. 260-32.6)
This invention relates to new compositions of matter and more particularly to new and useful compositions of matter comprising solutions or dopes of synthetic linear condensation polyesters. It is further concerned with new compositions of matter which are capable of being formed into useful articles such as ribbons, films, bristles, fibers, filaments and the like.
This application is a continuation-in-part of our copending application, Serial No. 593,358, filed June 25, 1956, now abandoned.
For the sake of simplicity, the present invention will be described as it is applied in the manufacture of fibers and filaments. However, the invention is not to be limited thereby except insofar as it may be limited by the appended claims.
Various methods are known for converting the polyesters described above into filaments and fibers, such as the so-called melt-spinning, wet-spinning and dry-spinning methods.
Melt-spinning comprises melting chips of a polyester on a heated grid and passing the melt through .a filter bed of small particles, such as sand, and the like. Subsequently, the melt is forced through a spinneret and the filaments so formed are cooled. However, melt-spinning has certain disadvantages such as the employment of high temperatures which makes the addition of plasticizers and modifying agents difiicult, because there is a tendency for the added agents to discolor and decompose.
In the dry-spinning method the polyester is dissolved in a solvent therefor and extruded through a spinneret in the usual manner. The solution is extruded into an atmosphere of inert gas which may be heated. The motion of the inert gaseous atmosphere, the extruded fiber and the application of heat all aid in disposing of the volatile solvent.
The wet-spinning method in which a solution of polyester is extruded into a bath containing a non-solvent for the polyester has a number of advantages over the melt-spinning method. For example, the wet-spinning method is generally more economical and can be carried out at lower temperatures. Therefore, plasticizers and other agents may be added with a minimum tendency toward discoloration and decomposition. Furthermore, certain types of plasticizers and modifying agents tend to be less compatible for blending in a melt at high temperatures, whereas they can be readily incorporated in a polyester solution at a low temperature. Solutions offer the further advantage in that they may be easily cast into films or coatings of uniform thickness. This is extremely diflicult with a molten composition because of its relatively high viscosity.
:The wet-spinning method, however, has not been employed commercially because of the lack of suitable s01- vents. Generally polyesters are insoluble in the more common organic solvents. From the standpoint of low cost, solvent power, non-corrosiveness and ease of recovery, there is a scarcity of suitable solvents for the more usual types of polyesters.
Accordingly, the principal object of the instant invention is the preparation of polyester solutions or dopes which are capable of being transformed into shaped articles.
Another object is to provide synthetic linear condensation polyester compositions in solutions which are stable and have non-gelation characteristics.
Another object of the invention is to prepare spinnable solutions of polyester compositions.
Other objects and advantages of the invention will be apparent from the following description.
The foregoing objects are accomplished by dissolving the synthetic linear condensation polyester in compounds having the general formula,
oona
wherein x is NH or a halogen. Among such compounds are ortho-anisidine, p-chloroanisole, m-anisidine, p-anisidine, o-chl-oroanisole, o-bromoanisole, and p-bromoanisole.
Solutions of high solids content and good stability can be prepared by mixing the polyester in the compounds mentioned hereinabove and heating to a temperature in a range of C. to the boiling point of the mixture. If desired, the mixture may be stirred while heating. However, stirring is not necessary to eifect solution, although it has been found that the polyester goes into solution more smoothly and evenly and with a greater rate of speed when stirring is employed. Whether stirring is employed or not, a miscible mixture of the synthetic linear condensation polyester is attained. The maximum solids concentration of the polyester that can be obtained in the solution and the viscosity of the solution depend upon the nature of the polyester, the solvent mixture and the temperature. In the manufacture of filaments and fibers a polyester having a molecular weight of at least 10,000 is employed in making a solution. Lower molecular weight polyesters may be utilized when the solution to be formed is to be used as a coating or as a lacquer. In prapering solutions or dopes suitable for spinning into filaments and fibers, 10 to 20 percent by weight of the polyester, based on the total weight of the solution, is suitable. While it is preferred to employ 10 to 20 percent by weight, based on the total Weight of the solution, of the polyester in the solvent when the solution is to be used for the preparation of fibers and filaments, it is to be understood that as little as 5 percent or less and as much as 25 percent or more of the polyester may be utilized when the solution is to be employed for other purposes, such as a coating or lacquer and the like, or when lower or higher molecular weight polyesters are to be dissolved in the new solvents of this invention. The amount of any specific polyester, which can be dissolved in the solvents of this invention, will be readily evident to those skilled in the art.
The synthetic linear condensation polyesters contemplated in the practice of the invention are those formed from dicarboxylic acids and glycols, and copolyesters or modifications of these polyesters and copolyesters. In a highly polymerized condition, these polyesters and copolyesters can be formed into filaments and the like and subsequently oriented permanently by cold drawing. The polyesters and copolyesters specifically useful in the instant invention are those resulting from heating one or more of the glycols of the series HO(CH ),,OH, in which n is an integer from 2 to 10, with one or more dicarboxylic acids or ester-forming derivatives thereof. Among the dicarboxylic acids and ester-forming derivatives thereof useful in the present invention there may be named terephthalic acid, isophthalic acid, sebacic acid, adipic acid, p-carboxyphenoacetic acid, succinic acid, p,pdicarboxybiphenyl, p,p-dicarboxycarbanilide, p,p-dicarcol and decamethylene glycol, etc.
wherein n is an integer from '1 to 4, and the aliphatic and cycloaliphatic aryl esters and half esters, ammonium and amine salts, and the acid halides of the above-named compounds and the like. Examples of the glycols which may be employed in practicing the instant invention are ethylene glycol, trirnethylene glycol, tetramethylene gly- Polyethylene terephthalate, however, is preferred because of the ready availability of terephthalic acid and ethylene glycol, from which it is made. It also has a relatively high melting point of about 250 through 255 C. and this property is particularly desirable in the manufacture of filaments in the textile industry.
Among the modified polyesters and copolyesters which are useful in the practice of the instant invention are the polyesters and copolyesters mentioned above modified with chain terminating groups having hydrophilic properties, such as the monofunctional ester-forming polyethers bearing the general formula,
wherein R is an alkyl group containing 1 to 18 carbon atoms or an aryl group containing 6 to carbon atoms, and m and n are integers from 2 to 22, and x is a whole number indicative of the degree of polymerization, that is, x is an integer from 1 to 100 or greater. Examples of such compounds are methoxypolyethylene glycol, ethoxypolyethylene glycol, n-propoxypolyethylene glycol, isopropoxypolyethylene glycol, butoxypolyethylene glycol, phenoxypolyethylene glycol, methoxypolypropylene glycol, methoxypolybutylene glycol, phenoxypolypropylene glycol, phenoxypolybutylene glycol, methoxypolymethyiene glycol, and the like. Suitable polyalkylvinyl ethers having one terminal hydroxyl group are the addition polymers prepared by the homopolymerization of alkylvinyl ethers wherein the alkyl group contains from 1 to 4 carbon atoms. Examples of such chain-terminating agents are polymethylvinyl ether, polyethylvinyl ether, polypropylvinyl ether, polybutylvinyl ether, polyisobutylvinyl ether, and the like. The chain-terminating agents or compounds may be employed in the preparation of the modified polyesters in amounts ranging from 0.05 mol percent to 4.0 mol percent, based on the amount of dicarboxylic acid or dialkyl ester thereof employed in the reaction mixttne. It is to be noted that when chainterminating agents are employed alone, i.e., without a chain-branching agent, the maximum amount that can be employed in the reaction mixture is 1.0 mol percent. Thus, unexpectedly, the addition of controlled amounts of chain-branching agents along with the chain-terminating agents allows the introduction of an increased amount of the latter into the polymer chain than is otherwise possible when employing the chain-terminating agents alone.
One will readily appreciate that the weight percent of chain-terminating agent which may be employed in this invention will vary with the molecular weight of the agent. The range of average molecular weights of the chainterminating agents suitable for use in this invention is from 500 to 5000, with those agents having a molecular weight in the range of 1000 to 3500 being preferred.
Materials suitable as chain-branching agents or crosslinking agents, which are employed to increase the viscosity or molecular weight of the polyesters, are the polyols which have a functionality greater than two, that is, they contain more than two functional groups, such as hydroxyl. Examples of suitable compounds are pentaerythritol; compounds having the formula:
wherein R is an alkylene group containing from 3 to 6 carbon atoms and n is an integer from 3 to 6, for example, glycerol, sorbitol, hexane trio1-l,2,6, and the like; compounds having the formula:
wherein R is an alkyl group containing from 2 to 6 carbon atoms, for example, tn'methylol ethane, trimethylol propane, and like compounds up to trimethylol hexane; and the compounds having the formula:
wherein n is an integer from 1 to 6. As examples of compounds having the above formula there may be named trimethylol benzene-1,3,5, triethylol benzene-1,3,5, tripropylol benzene-1,3,5, tributylol benzene-1,3,5, etc.
Aromatic polyfunctional acid esters may also be employed in this invention as chain-branching agents and particularly those having the formula:
law
and in which R, R and R" are alkyl groups containing 1 to 3 carbon atoms and R' is hydrogen or alkyl groups having 1 to 2 carbon atoms. As examples of compounds having the above formula there may be named trimethyl trimesate, tetramethyl pyromellitate, tetramethyl mello phonate, trimethyl hemimellitate, trimethyl trimelliate, tetramethyl prehnitate, and the like. In addition, there may be employed mixtures of the above esters which are obtained in practical synthesis. That is, in most instances when preparing any of the compounds having the above formula, other related compounds having the same formula may be present in small amounts as impurities. This does not afiect the compound as a chain-branching agent in the preparation of the modified polyesters and copolyesters described herein.
T he chain-branching agents or cross-linking agents may be employed in the preparation of the polyesters and copolyesters in amounts ranging from 0.05 mol percent to 2.4 mol percent, based on the amount of dicarboxylic acid or dialkyl ester thereof employed in the reaction mixture. The preferred range of chain-branching agent for use in the present invention is from 0.1 to 1.0 mol percent.
In the practice of the present invention, the calculated amounts of chain-terminating agent or chain-terminating agent and chain-branching agent or cross-linking agent are charged to the reaction vessel at the beginning of the first stage of the esterification reaction and the reaction proceeds as in any well-known esterification polymerization. The first step or stage of the reaction is carried out at atmospheric pressure and at a temperature in the range of C. to 250 C. and preferably between and 220 C. when from 0.001 to 1.0 percent by weight, based on the weight of the dicarboxylic acid or ester thereof, of a suitable esterification catalyst, such as manganous formate or zinc acetylacetonate, is employed. If desired, the reaction may be carried out at pressures above or below atmospheric. Methanol is evolved which is continuously removed by distillation. At the completion of the first stage, the excess glycol, if any, is distilled ofi prior to entering the second stage of the reaction.
In the second or polymerization stage, the reaction is conducted at reduced pressures and preferably in the presence of an inert gas, such as nitrogen, in order to prevent oxidation. This can be accomplished by maintaining a nitrogen blanket over the reactants, said nitrogen containing less than 0.003 percent oxygen. For optimum results, a pressure within the range of less than 1 mm. up to 5 mm. of mercury is employed. This reduced pressure is necessary to remove the free ethylene glycol that is formed during this stage of the reaction, the ethylene glycol being volatilized under these conditions and removed from the system. The polymerization step is c0nducted at a temperature in the range of 220 to 300 C. This stage of the reaction may be effected either in the liquid, melt or solid phase. In the liquid phase, particularly, reduced pressures must be employed in order to remove the free ethylene glycol which emerges from the polymer as a result of the condensation reaction.
In the preparation of the described polyesters, the first stage of the reaction takes place in approximately to 2 hours, when employing a suitable esterification catalyst. In the absence of a catalyst, times up to 6 hours may be necessary in order to complete this phase of the reaction. In the second stage, a reaction time of approximately 1 to 4 hours may be employed with a time of 1 to 3 hours being the optimum, depending on catalyst concentration, temperature, viscosity desired, amount of color allowable in the finished polymer, etc.
The modified linear condensation polyesters, produced in accordance with the present invention, have a specific viscosity in the range of 0.30 to 0.60, which represents the fiberand filament-forming polymers. It is to be understood, of course, that non-fiber-forming polyesters may be produced by means of the present invention, which have a specific viscosity greater or less than that reiterated above and such polyesters are useful, for example, in the manufacture of coating compositions, lacquers, molding compositions, and the like. This specific viscosity range and variations thereof also are applicable to the unmodified polyesters, such as polyethylene terephthalate. The specific viscosity range of the fiber-forming polymers, that is, from 0.3 to about 0.6, indicates high molecular weight polymers of from about 10,000 to about 50,000 molecular weight.
If it is desired to produce shaped articles from the polyester solutions of the present invention which have a modified appearance or modified properties, various agents to accomplish these effects may be added to the polyester solutions of this invention prior to the fabrication of the articles without any ill efiects thereon. Such added agents might be plasticizers, pigments, dyes, anti-static agents, fire-retarding agents, etc.
The following examples are intended to illustrate the new compositions of the invention more fully, but are not intended to limit the scope of the invention, for it is possible to efiect many modifications therein. In the examples, all parts and percents are by weight unless otherwise indicated.
Example I 9 grams of o-anisidine and 1 gram of polyethylene terephthalate were mixed together and warmed with stirring to 180 C. where the polymer readily dissolved yielding a clear fluid solution suitable for both wet and dry spinning. On cooling, the solution solidified at 85 C. but was easily redissolved upon the application of heat.
Example 11 There was charged to a reaction vessel 82 grams of dimethyl terephthalate, 106.2 grams of ethylene glycol (approximately 88 ml.) and 8.2 grams of ethoxypolyethylene glycol having an average molecular weight of about 3050 (0.5 mol percent based on the mols of dimethyl terephthalate). Subsequently, 40 mg. of manganous formate was added to the reaction vessel. The reactants were Will mixed and heated at 177 C. until solution was effected. The mixture was maintained at this temperature for 90 minutes to bring about the ester'interchange reaction. Thereafter, the temperature was raised to 225 C. to remove excess ethylene glycol and maintained at that temperature under a vacuum of less than 1 mm. of mercury for 3 hours to elfect polymerization. There was obtained a high molecular weight polyester having a melting point of about 255 C. and a specific viscosity of about 0.3 at 25 C. calculated in a 2 to 1 mixture of phenol-trichlorophenol containing 0.5 percent by weight of polymer. 1 gram of the polyester so prepared and 9 grams of o-anisidine were mixed together and warmed with stirring to 180 C. Where the polymer readily dissolved yielding a clear fluid solution. On cooling, the solution solidified at 90 C. but was easily redissolved upon the application of heat. The solution was suitable for the formation of fibers by both wet and dry spinning methods.
Example III 9 grams of p-chloroanisole and 1 gram of polyethylene terephthalate were mixed together and warmed with stirring to 185 C. where the polymer readily dissolved yielding a clear fluid solution suitable for both wet and dry spinning. On cooling, the solution solidified at C. but was easily redissolved upon the application of heat.
Example IV A polyester formed as in Example II but with approximately 16.4 grams of ethoxypolyethylene glycol (that is, about 1 mol percent based on the rmols of dimethyl terephthalate) were mixed with 9 grams of p-chloroanisole and warmed with stirring to 185 C. where the polymer readily dissolved yielding a clear fluid solution. On cooling, the solution became solid at about 125 C. but was easily redissolved upon the application of heat.
Example V 9 grams of o-anisidine and 1 gram of the polyester employed in Example IV were mixed together and warmed with stirring to 180 C. where the polymer readily dissolved yielding a clear fluid solution suitable for both Wet and dry spinning. The solution was stable at temperatures above 85 C.
Example VII There was charged to a reaction vessel 1650 grams of dimethyl terephthalate, 1980 grams (approximately 1775 ml.) of ethylene glycol and 165 grams of methoxypolyethylene glycol having an average molecular Weight of abopt 2000 (1.0 mol percent based on the mols of dimethyl terephthalate). There was also added to the reaction vessel 1.32 grams of pentaerythritol. Subse, quently, 1.07 grams of zinc acetylacetonate were added to the reaction vessel. The reactants were well mixed and heated for about 90 minutes at atmospheric pressure and at a temperature gradually raised from C. to 198 C. until solution was effected. During this time methyl alcohol which was formed in the reaction was removed by distillation. Subsequently, the reactants were heated for about 45 minutes under atmospheric pressure at a temperature which was gradually raised from 198 C. to 240 C. to remove excess ethylene glycol. Then the temperature was raiesd from 240 C. to about 280 C. over a period of about minutes while the pressure was gradually decreased from atmospheric pressure to about 1 mm. of mercury. The reaction mixture was subjected for about 1 /2 hours to 280 C. and about 1 mm. of mercury to efiect polymerization. There was obtained a high molecular weight polyester having a melting point of about 255 C. and a specific viscosity of 0.50 at 25 C. calculated in a 2 to 1 mixture of phenol-trichlorophenol containing 0.5 percent by weight of polymer. 0.5 gram of the polyester so prepared and 9.5 grams of p-chloroanisole were mixed together and heated. The polyester began dissolving at about 125 C. The solution was complete at 175 C. On cooling, a small amount of precipitate formed at around 160 C. The solution became turbid around 140 C. and solidified at 135 C.
Example VIII 2 grams of the polyester prepared in Example ViI were mixed with 8 grams of p-chloroanisole. The polyester was practically completely dissolved at about 175 C. The solution so formed was very viscous and suitable for the preparation of films.
Example IX 2 grams of the polyester formed by the procedure of Example VII were mixed with 8 grams of o-anisidine. The polyester began to dissolve at about 140 C. Solution was complete at 170 C. As the solution began to cool, a slight precipitate formed at about 140 C. At 130 C. the solution became turbid and thick. Upon falling to 125 C. it became semi-solid. At about 170 C. the solution was clear, colorless and viscous. It was suitable for the formation of fibers.
Example X 2.5 grams of the polyester prepared according to the procedure of Example VII and 7.0 grams of o-anisidine were mixed together and heated with stirring to about 170 C. where solution was formed. Upon cooling, precipitation of the polyester was noted at about 155 C. At 140 C. the solution became turbid and thick and at 135 C. it was semi-solid. The solution was suitable for the formation of films at about 170 C.
The polyester compositions of this invention can be usefully employed in the coating field, for example, in the coating of textile fabrics. Thus, a fabric can be coated and/or impregnated with the polyester solutions described herein and then treated, that is soaked, in a non-solvent for the polyester in order to precipitate the polyester in and on the fabric. Metals, paper and impervious films may also be coated with the polyester compositions of this invention by conventional and wellknown procedures.
One of the principal advantages of the instant invention is that it provides polyester compositions which are readily convertible to useful shaped articles by the wet or dry spinning methods which are more economical than the melt-spinning method. Numerous other advantages of this invention will be apparent to those skilled in the art from reading the instant description.
As many apparently widely different embodiments of this invention may be made without departing from the spirit and scope thereof, it is to be understood that the same is not to be limited to the specific embodiments thereof, except as defined in the appended claims.
We claim:
1, A new composition of matter comprising a solution of a synthetic linear condensation polyester dissolved in a solvent having the general formula,
wherein R is selected from the group consisting of alkyl groups containing 1 to 18 carbon atoms and aryl groups containing 6 to 10 carbon atoms, In and n are integers from 2 to 22, and x is an integer from 1 to 100, and (C) the polyesters of (B) containing 0.05 mol percent to 4.0 mol percent of a chain terminator based on the total weight of said dicarboxylic acid modified by 0.05 mol percent to 2.4 mol percent based on the total weight of said dicarboxylic acid, of a chain-branching agent comprising pentaerythritol.
2. A new composition of matter as defined in claim 1 wherein the polyester is polyethylene terephthalate.
3. A new composition of matter as defined in claim 1 wherein the solvent is o-anisidine.
4. A new composition of matter as defined in claim wherein the solvent is p-chloroanisole.
5. A new composition of matter as defined in claim wherein the solvent is m-anisidine.
6. A new composition of matter as defined in claim 1 wherein the solvent is p-anisidine.
7.1 new composition of matter as defined in claim 1 wherein the solvent is o-chloroanisole.
8. A new composition of matter as defined in claim 1 wherein the chain terminator is ethoxypolyethylene glycol.
9. A new composition of matter as defined in claim 1 wherein the chain terminator is methoxypolyethylene glycol.
10. A new composition of matter as defined in claim 1 wherein the chain terminator is propoxypolyethylene glycol.
11. A new composition of matter as defined in claim 1 wherein the cross-linking agent is pentaerythritol.
12. A new composition of matter comprising a solution of a synthetic linear condensation polyester dissolved in a solvent having the general formula,
wherein x is selected from the group consisting of -NH and chloro, said polyester being selected from the group consisting of (A) polyesters formed by the reaction of at least one dicarboxylic acid selected from the group consisting of aromatic dicarboxylic acids and saturated aliphatic dicarboxylic acids and at least one glycol of the series HO(CH OI-I wherein n is an integer from 2 to 10, (B) the polyesters of (A) modified by 0.05 mol percent to 1.0 mol percent, based on the total weight of said dicarboxylic acid, of a chain terminator having the formula,
(I) 2) m X(CH2) n' wherein R is selected from the group consisting of alkyl groups containing 1 to 18 carbon atoms and aryl groups containing 6 to 10 carbon atoms, m and n are integers from 2 to 22, and x is an integer from 1 to 100, and (C) the polyesters of (B) containing 0.05 mol percent to 4.0 mol percent of a chain terminator based on the total weight of said dicarboxylic acid modified by 0.05 mol percent to 2.4 mol percent based on the total weight of said dicarboxylic acid, of a chain-branching agent comprising pentaerythritol, said solvent being employed in a range of 80 to 90 percent, based on the total weight of the composition.
13. A new fiber-forming composition of matter com- OCH;
wherein x is selected from the group consisting of NH and chloro.
No references cited.
Claims (1)
1. A NEW COMPOSITION OF MATTER COMPRISING A SOLUTION OF A SYNTHETIC LINEAR CONDENSATION POLYESTER DISSOLVED IN A SOLVENT HAVING THE GENERAL FORMULA,
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL124012D NL124012C (en) | 1958-10-03 | ||
BE583162D BE583162A (en) | 1958-10-03 | ||
NL243965D NL243965A (en) | 1958-10-03 | ||
US765024A US3063956A (en) | 1958-10-03 | 1958-10-03 | Polyester solution in an aromatic ether solvent |
GB33067/59A GB951438A (en) | 1958-10-03 | 1959-09-29 | Polyester compositions |
FR806447A FR1238038A (en) | 1958-10-03 | 1959-09-30 | Spinnable polyester solutions |
CH7885459A CH429166A (en) | 1958-10-03 | 1959-09-30 | New composition of spinnable polyesters and method of preparation |
DEC19903A DE1129687B (en) | 1958-10-03 | 1959-10-02 | Use of methoxyaryl compounds as solvents for polyester |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US765024A US3063956A (en) | 1958-10-03 | 1958-10-03 | Polyester solution in an aromatic ether solvent |
Publications (1)
Publication Number | Publication Date |
---|---|
US3063956A true US3063956A (en) | 1962-11-13 |
Family
ID=25072429
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US765024A Expired - Lifetime US3063956A (en) | 1958-10-03 | 1958-10-03 | Polyester solution in an aromatic ether solvent |
Country Status (7)
Country | Link |
---|---|
US (1) | US3063956A (en) |
BE (1) | BE583162A (en) |
CH (1) | CH429166A (en) |
DE (1) | DE1129687B (en) |
FR (1) | FR1238038A (en) |
GB (1) | GB951438A (en) |
NL (2) | NL124012C (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3305534A (en) * | 1963-01-28 | 1967-02-21 | Monsanto Co | Zinc chelates as catalysts in the production of polyesters |
US3329656A (en) * | 1966-09-08 | 1967-07-04 | Monsanto Co | Zinc chelates as catalysts in the production of polyesters |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE950030C (en) * | 1951-06-21 | 1956-10-04 | Glanzstoff Ag | Process for dissolving and cleaning polyethylene terephthalate |
DE969988C (en) * | 1953-03-03 | 1958-09-04 | Hoechst Ag | Solvents and plasticizers |
DE939289C (en) * | 1953-03-07 | 1956-02-16 | Hoechst Ag | Solvents and plasticizers |
-
0
- BE BE583162D patent/BE583162A/xx unknown
- NL NL243965D patent/NL243965A/xx unknown
- NL NL124012D patent/NL124012C/xx active
-
1958
- 1958-10-03 US US765024A patent/US3063956A/en not_active Expired - Lifetime
-
1959
- 1959-09-29 GB GB33067/59A patent/GB951438A/en not_active Expired
- 1959-09-30 FR FR806447A patent/FR1238038A/en not_active Expired
- 1959-09-30 CH CH7885459A patent/CH429166A/en unknown
- 1959-10-02 DE DEC19903A patent/DE1129687B/en active Pending
Non-Patent Citations (1)
Title |
---|
None * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3305534A (en) * | 1963-01-28 | 1967-02-21 | Monsanto Co | Zinc chelates as catalysts in the production of polyesters |
US3329656A (en) * | 1966-09-08 | 1967-07-04 | Monsanto Co | Zinc chelates as catalysts in the production of polyesters |
Also Published As
Publication number | Publication date |
---|---|
FR1238038A (en) | 1960-08-05 |
DE1129687B (en) | 1962-05-17 |
NL243965A (en) | |
CH429166A (en) | 1967-01-31 |
NL124012C (en) | |
GB951438A (en) | 1964-03-04 |
BE583162A (en) |
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